Document 0268 DOCN M9590268 TI Characterisation of p53 responsive regions in the HIV-1 LTR. DT 9509 AU Tanskanen E; Braithwaite A; Doherty R; Virus Interactions Laboratory, Macfarlane Burnet Centre for; Medical Research, Fairfield, Vic. SO Annu Conf Australas Soc HIV Med. 1994 Nov 3-6;6:254 (unnumbered poster). Unique Identifier : AIDSLINE ASHM6/95291831 AB Transcriptional control over genes of HIV and other retroviruses is exerted by regulatory factors via responsive elements in the long terminal repeat (LTR). Functional p53 is a nuclear phosphoprotein which has a tumour suppressor role in dividing cells. p53 can act as a transcription factor, transactivating promoters containing the consensus p53 binding site while suppressing some promoters not containing this site. We and others have observed that the tumour suppressor protein p53 is able to repress HIV-1 LTR directed transcription. To characterise the regions of the HIV-1 LTR that are responsive to p53 mediated repression we have completed a series of transfection experiments with CAT reporter constructs containing 18bp sequential deletions of the HIV-1 LTR in the presence and absence of over expressed p53. Preliminary results suggest that the region containing the TATA box and most 3' SP1 site is responsive to repression by p53 and we have also observed that the region from nt-147 to nt-93 relative to transcription initiation may also be involved. Using in vitro transcribed and translated p53 we have been unable to detect direct p53 binding to these regions of the LTR and are now investigating the possibility that p53 action is mediated by interaction between proteins either in cooperative binding or by acting as an inhibitor of transcription factors essential for HIV-1 transcription. DE Gene Expression Regulation, Viral/PHYSIOLOGY Human HIV Long Terminal Repeat/*GENETICS HIV-1/*GENETICS Protein p53/*GENETICS Repressor Proteins/GENETICS Transcription, Genetic Transfection MEETING ABSTRACT SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).